<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>15060289041585</udiDi>
    <basicUdiDi>B-15060289041585</basicUdiDi>
    <tradeName>15060289041585</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Unimax Medical Systems Inc.</manufacturerName>
    <manufacturerSrn>TW-MF-000008895</manufacturerSrn>
    <authorisedRepresentativeName>mdi Europa GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000006218</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>H900803</emdnCode>
    <emdnDescription>SINGLE-USE SUTURE PASSER AND PORT/FASCIAL CLOSURE SYSTEMS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LM120C2 / FCL200003</reference>
    <placedOnMarketCountry>Greece</placedOnMarketCountry>
    <lastUpdated>2026-06-17T01:44:13.620Z</lastUpdated>
  </row>
  <row>
    <udiDi>15060289040786</udiDi>
    <basicUdiDi>B-15060289040786</basicUdiDi>
    <tradeName>15060289040786</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Unimax Medical Systems Inc.</manufacturerName>
    <manufacturerSrn>TW-MF-000008895</manufacturerSrn>
    <authorisedRepresentativeName>mdi Europa GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000006218</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>H900803</emdnCode>
    <emdnDescription>SINGLE-USE SUTURE PASSER AND PORT/FASCIAL CLOSURE SYSTEMS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LM120C / FCL100001</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-06-17T01:39:52.196Z</lastUpdated>
  </row>
</eudamedExport>